| 注册
首页|期刊导航|武警医学|髓样细胞触发受体-1基因rs9471535单核苷酸多态性与男性早发冠心病的相关性

髓样细胞触发受体-1基因rs9471535单核苷酸多态性与男性早发冠心病的相关性

杨勇 孟涛疆 马东星 刘英 沈志奇 黄洁 赵清 王冉冉 杨长春

武警医学2019,Vol.30Issue(2):97-100,104,5.
武警医学2019,Vol.30Issue(2):97-100,104,5.

髓样细胞触发受体-1基因rs9471535单核苷酸多态性与男性早发冠心病的相关性

Relationships between TREM-1 gene polymorphism and susceptibility to male premature coronary artery disease

杨勇 1孟涛疆 2马东星 1刘英 1沈志奇 1黄洁 1赵清 1王冉冉 1杨长春1

作者信息

  • 1. 解放军总医院第三医学中心心血管内科 100039 北京
  • 2. 解放军联勤保障部队三亚康复疗养中心 572000
  • 折叠

摘要

Abstract

Objective To explore the correlations between gene polymorphisms of triggering receptor expressed on myeloid cells-1 (TREM-1) rs9471535 and susceptibility to male premature coronary artery disease (PCAD). Methods Between August 2015 and January2017, male inpatients aged 55 or above, treated at the Department of Cardiology of our hospital, and identified by coronary angiography or CTA with CAD (PCAD group) or without CAD (control group), were enrolled into this study. The DNA kit was used to extract DNA from peripheral venous blood, and polymerase chain reaction-ligase detection reaction (PCR-LDR) technology was used to identify the TREM-1 gene polymorphisms. The frequencies of genotypes and alleles of rs9471535 were calculated and binary logistic regression was used to analyze the relationships between rs9471535 polymorphisms and susceptibility to PCAD. Results The percentages of patients with hypertension (57.0%), diabetes (21. 5%), hyperlipidemia (59. 5%) or with smoking history (74. 4%) were significantly higher in the PCAD group than those in the control group (P < 0. 05). The frequencies of genotypes TT (46. 3%), CT (50. 4%) and CC (3. 3%) of rs9471535 in the PCAD group were significantly different from those of the control group, which were 51. 0%, 38. 3%, and 10. 7% respectively (P = 0. 017).According to univariate analysis with binary logistic regression, as compared with TT genotype, the distribution of CC genotype was not significantly different between the two groups (P = 0. 059, OR = 0. 340, 95% CI= 0. 111-1. 041). However, after adjustment of traditional risk factors (age, hypertension, diabetes, hyperlipidemia and smoking), carriers of CC genotype had lower risk of PCAD (P = 0. 011, OR = 0. 180, 95% CI =0. 048-0. 679). Conclusions The TREM-1 gene rs9471535 polymorphism may have correlations with the occurrence of male premature CAD. Individuals with CT and TT genotypes may be more vulnerable to premature CAD than those carrying CC genotype that may play a protective role in male PCAD.

关键词

早发冠心病/TREM-1基因/rs9471535/单核苷酸多态性

Key words

PCAD/TREM-1/rs9471535/single nucleotide polymorphism

分类

医药卫生

引用本文复制引用

杨勇,孟涛疆,马东星,刘英,沈志奇,黄洁,赵清,王冉冉,杨长春..髓样细胞触发受体-1基因rs9471535单核苷酸多态性与男性早发冠心病的相关性[J].武警医学,2019,30(2):97-100,104,5.

基金项目

原武警总医院科研创新预研资助项目(WZ2015013) (WZ2015013)

武警医学

OACSTPCD

1004-3594

访问量0
|
下载量0
段落导航相关论文